Pharma Technical Writer: GMP Docs & SOPs for Facilities

A leading biopharmaceutical firm is seeking an experienced Technical Writer to support documentation efforts in Frederick, MD. The role involves creating and maintaining controlled documentation for facility operations and ensuring compliance with GMP standards. Candidates should have over 3 years of experience in technical writing, proficiency with document management systems, and strong organizational skills. A Bachelor's degree in a related field is required. Competitive salary and comprehensive benefits are offered. #J-18808-Ljbffr